Lincare Recalls Ceftazidime IV Bags Due to Sterility Concerns
Lincare, Inc. is recalling compounded Ceftazidime IV bags because the sterility of the product is not assured.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, which corresponds to a Severe severity score according to the rubric, particularly given the risk of infection from non-sterile medical products.
Plain-English summary
Lincare, Inc. is recalling 15 bags of compounded Ceftazidime 2 gm / NS 50mL. The product was compounded by United Medical IV Center in Little Rock, Arkansas, on May 28, 2015, with a discard after date of June 11, 2015.
The recall was initiated because the sterility of the product is not assured. This lack of assurance regarding sterility poses a potential risk to patients using the medication.
The affected product was distributed in the United States, including Arkansas. Consumers and healthcare providers should stop using the recalled product and contact their healthcare provider or Lincare, Inc. for further instructions.
The recalled product
- Product
- Ceftazidime 2 gm / NS 50mL, Qty: 15 50 mL Bags, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
- Manufacturer
- Lincare, Inc.
- Category
- Drug — Compounded IV
- Hazard
- Affected units
- 15
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Compounded on 05/28/15
- Discard After: 06/11/15
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 54 recalled by Lincare, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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